FAM111B Polyclonal Antibody, 100ul Nucleic Acid Isolation & Purification Loss or altered expression of

Loss or altered expression of this gene has been associated with the pathogenesis of a variety of cancers

a repair-deficient mutant that exhibits hypersensitivity to a number of different DNA-damaging agents

phosphorylate and repress the activity of E47

A regulator gene for tyrosine aminotransferase is X-linked

FAM111B Polyclonal Antibody, 100ul Nucleic Acid Isolation & Purification Loss or altered expression ofFAM111B encodes a protein with a trypsin like cysteine serine peptidase domain in the C terminus. Mutations in this gene are associated with an autosomal dominant form of hereditary fibrosing poikiloderma (HFP). Affected individuals display mottled pigmentation, telangiectasia, epidermal atrophy, tendon contractures, and progressive pulmonary fibrosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. A paralog